Georgia Code Title 31. Health § 31-52-3

(1) “Eligible patient” means a person who meets the requirements of Code Section 31-52-4.

(2) “Investigational drug, biological product, or device” means a drug, biological product, or device which has successfully completed Phase I of a federal Food and Drug Administration approved clinical trial but has not yet been approved for general use by the federal Food and Drug Administration and currently remains under investigation in a federal Food and Drug Administration approved clinical trial.

(3) “Physician” means a person licensed to practice medicine pursuant to Article 2 of Chapter 34 of Title 43.

(4) “Terminal illness” means a disease that, without life-sustaining procedures, will result in death in the near future and is not considered by a treating physician to be reversible even with administration of current federal Food and Drug Administration approved and available treatments.

(5) “Written informed consent” means a written document that: